Canonical Allele Identifier: CA2450719201

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687487C= , CM000685.2:g.108687487C=	GRCh38
NC_000023.10:g.107930717C= , CM000685.1:g.107930717C=	GRCh37
NC_000023.9:g.107817373C=	NCBI36
NG_011977.1:g.252564C=
NG_011977.2:g.252564C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4321C= MANE Select	ENSP00000331902.7:p.Arg1441=
ENST00000361603.7:c.4303C=	ENSP00000354505.2:p.Arg1435=
ENST00000510690.2:n.815C=
ENST00000328300.10:c.4321C=	ENSP00000331902.6:p.Arg1441=
ENST00000361603.6:c.4303C=	ENSP00000354505.2:p.Arg1435=
ENST00000489230.1:n.724C=
ENST00000515658.1:c.117C=
NM_000495.4:c.4303C=	NP_000486.1:p.Arg1435=
NM_033380.2:c.4321C=	NP_203699.1:p.Arg1441=
XM_005262070.2:c.4312C=	XP_005262127.1:p.Arg1438=
XM_006724616.2:c.4321C=	XP_006724679.1:p.Arg1441=
XM_011530849.1:c.3997C=	XP_011529151.1:p.Arg1333=
XM_011530851.1:c.1894C=	XP_011529153.1:p.Arg632=
XM_011530849.2:c.4336C=	XP_011529151.2:p.Arg1446=
XM_017029259.2:c.4327C=	XP_016884748.1:p.Arg1443=
XM_017029260.1:c.4318C=	XP_016884749.1:p.Arg1440=
XM_017029263.2:c.2656C=	XP_016884752.1:p.Arg886=
NM_000495.5:c.4303C=	NP_000486.1:p.Arg1435=
NM_033380.3:c.4321C= MANE Select	NP_203699.1:p.Arg1441=